rs121908590

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs121908590(G;T)

Make rs121908590(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

5045270

Gene

KCNA5

is a	snp
is	mentioned by
dbSNP	rs121908590
dbSNP (classic)	rs121908590
ClinGen	rs121908590
ebi	rs121908590
HLI	rs121908590
Exac	rs121908590
Gnomad	rs121908590
Varsome	rs121908590
LitVar	rs121908590
Map	rs121908590
PheGenI	rs121908590
Biobank	rs121908590
1000 genomes	rs121908590
hgdp	rs121908590
ensembl	rs121908590
geneview	rs121908590
scholar	rs121908590
google	rs121908590
pharmgkb	rs121908590
gwascentral	rs121908590
openSNP	rs121908590
23andMe	rs121908590
SNPshot	rs121908590
SNPdbe	rs121908590
MSV3d	rs121908590
GWAS Ctlg	rs121908590

Max Magnitude

0

OMIM	176267
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908590(A;A) rs121908590(T;T)
Alt	rs121908590(A;A) rs121908590(T;T)
Reference	Rs121908590(G;G)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	KCNA5
CLNDBN	Atrial fibrillation, familial, 7
Reversed	0
HGVS	NC_000012.11:g.5154436G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014411.26,